Myanmar FDA registration 5e9e8318134f5a5a91fdb2fb84668d17

PTFE Guide Wire

Myanmar·INDOVASIVE·Biorad Medisys Pvt. Ltd.·Registered July 26, 2022

Device classification

Brand Name: INDOVASIVE

Registration information

Analysis ID: 5e9e8318134f5a5a91fdb2fb84668d17
Registration Date: July 26, 2022

Manufacturer

Name: Biorad Medisys Pvt. Ltd.

Authorized Representative

Name: NI LAY NAING COMPANY LIMITED

About this record

Access comprehensive regulatory information for PTFE Guide Wire in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5e9e8318134f5a5a91fdb2fb84668d17 and manufactured by Biorad Medisys Pvt. Ltd.. The device was registered on July 26, 2022.

This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.